Test Utilization Discussions: Should the Qualitative Serum Pregnancy Test Be Considered Obsolete?
Rapid testing for the qualitative detection of human chorionic gonadotropin (hCG) in urine or serum using point-of care (POC) test devices is frequently performed in health care settings to identify a possible pregnancy. Qualitative urine hCG tests are attractive because the urine sample requires no special processing and the tests are granted waived status by the Clinical Laboratory Improvement Amendments (CLIA). As such, testing can truly be performed at the POC by any health care provider. In contrast, qualitative serum hCG tests are categorized by CLIA as moderately complex because they require the collection of a whole blood specimen that must be centrifuged before testing to obtain the serum sample. The need to perform qualitative hCG testing in serum has been questioned for several reasons. First, owing to the sample type, testing cannot be performed at the POC. Second, clinical laboratories are often able to perform quantitative serum hCG tests that have relatively short analytic times (10-20 minutes). Third, quantitative hCG tests can measure hCG at a concentration lower than the detection thresholds claimed by qualitative tests (~1 vs 10-25 IU/L, respectively). Fourth, because the only clinical use of a qualitative serum hCG test is to detect (or rule out) a possible pregnancy, it can be argued that the most analytically sensitive test available (ie, quantitative) should be used.
